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1دورية أكاديمية
المؤلفون: Kyung Seok Oh, Jae Won Roh, Sun Young Joo, Kunhi Ryu, Jung Ah Kim, Se Jin Kim, Seung Hyun Jang, Young Ik Koh, Da Hye Kim, Hye-Youn Kim, Murim Choi, Jinsei Jung, Wan Namkung, Joo Hyun Nam, Jae Young Choi, Heon Yung Gee
المصدر: Experimental and Molecular Medicine, Vol 55, Iss 4, Pp 844-859 (2023)
مصطلحات موضوعية: Medicine, Biochemistry, QD415-436
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2092-6413
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2دورية أكاديمية
المؤلفون: Jinsei Jung, Haiyue Lin, Young Ik Koh, Kunhi Ryu, Joon Suk Lee, John Hoon Rim, Hye Ji Choi, Hak Joon Lee, Hye-Youn Kim, Seyoung Yu, Hyunsoo Jin, Ji Hyun Lee, Min Goo Lee, Wan Namkung, Jae Young Choi, Heon Yung Gee
المصدر: Experimental and Molecular Medicine, Vol 51, Iss 8, Pp 1-12 (2019)
مصطلحات موضوعية: Medicine, Biochemistry, QD415-436
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Jinsei Jung, Hyun Been Choi, Young Ik Koh, John Hoon Rim, Hye Ji Choi, Sung Huhn Kim, Jae Hyun Lee, Jieun An, Ami Kim, Joon Suk Lee, Sun Young Joo, Seyoung Yu, Jae Young Choi, Tong Mook Kang, Heon Yung Gee
المصدر: Scientific Reports, Vol 8, Iss 1, Pp 1-11 (2018)
مصطلحات موضوعية: Non-syndromic Hearing Loss, Autosomal Dominant Non-syndromic Deafness (DFNA2), KCNQ Channels, Retigabine, Strong Dominant-negative Effect, Medicine, Science
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2045-2322
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4
المؤلفون: Doo-Yi Oh, Heon Yung Gee, Sang-Yeon Lee, Ami Kim, Jieun An, Bong Jik Kim, Na-Young Yi, Jin Hee Han, Min Young Kim, Seungmin Lee, Chung Lee, Nahyun Kim, Young Ik Koh, Eunku Kim, Hyun Been Choi, Hyun Sung Cho, Woong-Yang Park, Byung Yoon Choi, Tong Mook Kang, Mina Park, Il Soon Choi, Nayoung K.D. Kim
المصدر: Experimental & Molecular Medicine
مصطلحات موضوعية: Male, Phosphatidylinositol 4,5-Diphosphate, 0301 basic medicine, Patch-Clamp Techniques, Genotype, Concatemer, Clinical Biochemistry, Mutant, Mutation, Missense, Context (language use), Deafness, Biology, Biochemistry, Article, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Protein Domains, Genetics research, Humans, Homomeric, Molecular Biology, KCNQ Potassium Channels, HEK 293 cells, Translational research, Phenotype, Potassium channel, Pedigree, Cell biology, HEK293 Cells, 030104 developmental biology, chemistry, Potassium, Molecular Medicine, Female, 030217 neurology & neurosurgery, KCNQ4
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5
المؤلفون: Young Ik Koh, Kyung Seok Oh, Jung Ah Kim, Byunghwa Noh, Hye Ji Choi, Sun Young Joo, John Hoon Rim, Hye-Youn Kim, Dong Yun Kim, Seyoung Yu, Da Hye Kim, Sang-Guk Lee, Jinsei Jung, Jae Young Choi, Heon Yung Gee
مصطلحات موضوعية: otorhinolaryngologic diseases, Cell Biology, Molecular Biology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55ea9fe3d6584527441a6ff0d26d3b37
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6
المؤلفون: Hye Ji Choi, Kyung Seok Oh, Heon Yung Gee, Sun Young Joo, Jae Young Choi, Seyoung Yu, Young Ik Koh, Richard J.H. Smith, John Hoon Rim, Daniel Walls, Jinsei Jung, Jung Ah Kim, Hye-Youn Kim, Jee Eun Yoo, Da Hye Kim
المصدر: Hum Genet
مصطلحات موضوعية: Genotype, Hearing loss, Hearing Loss, Sensorineural, Biology, Deafness, Article, otorhinolaryngologic diseases, Genetics, medicine, Humans, Functional studies, Hearing Loss, Genetics (clinical), Exome sequencing, Arthrogryposis, Extracellular Matrix Proteins, LCCL domain, Phenotype, Human genetics, Pedigree, Cohort, Mutation, Phenotype genotype, medicine.symptom
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::001a7020b70405df02e22bb7b56ced5e
https://europepmc.org/articles/PMC8924011/ -
7
المؤلفون: Hye-Youn Kim, Seung-Tae Lee, Jinsei Jung, Sun Young Joo, Jung Ah Kim, John Hoon Rim, Da Hye Kim, Jae Young Choi, Jee Eun Yoo, Young Ik Koh, Byunghwa Noh, Kyumin Kim, Kyung Seok Oh, Jinwoong Bok, Heon Yung Gee, Min Goo Lee
المصدر: Human genetics. 141(3-4)
مصطلحات موضوعية: Oncology, Adult, medicine.medical_specialty, Candidate gene, Hearing loss, Hearing Loss, Sensorineural, Hearing Tests, Confounding, Audiogram, Biology, Ligands, Molecular medicine, Human genetics, Pedigree, Internal medicine, Exome Sequencing, Genetics, medicine, Humans, Medical diagnosis, medicine.symptom, Pathology, Molecular, Hearing Loss, Genetics (clinical), Exome sequencing
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8
المؤلفون: Seyoung Yu, Ji Hyun Lee, Min Goo Lee, Joon Suk Lee, John Hoon Rim, Haiyue Lin, Jae Young Choi, Heon Yung Gee, Jinsei Jung, Hyunsoo Jin, Wan Namkung, Hye Youn Kim, Hye Ji Choi, Young Ik Koh, Kunhi Ryu, Hak Joon Lee
المصدر: Experimental and Molecular Medicine, Vol 51, Iss 8, Pp 1-12 (2019)
Experimental & Molecular Medicineمصطلحات موضوعية: 0301 basic medicine, Clinical Biochemistry, lcsh:Medicine, Deafness, medicine.disease_cause, computer.software_genre, Biochemistry, 0302 clinical medicine, Gene Frequency, Hearing, Cricetinae, Databases, Genetic, Missense mutation, lcsh:QD415-436, Mutation, education.field_of_study, KCNQ Potassium Channels, Database, Potassium channel activity, Mechanisms of disease, 030220 oncology & carcinogenesis, Molecular Medicine, medicine.symptom, Ion Channel Gating, KCNQ4, Hearing loss, Population, Neurophysiology, CHO Cells, Biology, Article, lcsh:Biochemistry, 03 medical and health sciences, Cricetulus, otorhinolaryngologic diseases, medicine, Animals, Humans, Genetic variation, Hearing Loss, education, Molecular Biology, Allele frequency, Public Sector, lcsh:R, Minor allele frequency, HEK293 Cells, 030104 developmental biology, computer
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9
المؤلفون: Heon Yung Gee, Tong Mook Kang, Seyoung Yu, Sun Young Joo, Joon Suk Lee, John Hoon Rim, Young Ik Koh, Jinsei Jung, Sung Huhn Kim, Jae Young Choi, Jae Hyun Lee, Ami Kim, Hyun Been Choi, Jieun An, Hye Ji Choi
المصدر: Scientific Reports, Vol 8, Iss 1, Pp 1-11 (2018)
Scientific Reportsمصطلحات موضوعية: 0301 basic medicine, Adult, Male, Hearing loss, Science, Mutant, DNA Mutational Analysis, Deafness, Autosomal Dominant Non-syndromic Deafness (DFNA2), medicine.disease_cause, Article, 03 medical and health sciences, chemistry.chemical_compound, Exome Sequencing, medicine, Missense mutation, Humans, Amino Acid Sequence, Child, Exome sequencing, Non-syndromic Hearing Loss, Strong Dominant-negative Effect, Mutation, Multidisciplinary, KCNQ Potassium Channels, Retigabine, HEK 293 cells, Molecular biology, Pedigree, 030104 developmental biology, HEK293 Cells, chemistry, Medicine, Female, medicine.symptom, KCNQ Channels, KCNQ4, HeLa Cells
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10
المؤلفون: Heon Yung Gee, Seungyeon Lee, Joon Suk Lee, Do Hyeon Cha, Sun Young Joo, Ji Hyun Lee, John Hoon Rim, Dong Hoon Shin, Jinsei Jung, Hye Ji Choi, Min Goo Lee, Young Ik Koh, Jae Young Choi, Seyoung Yu
المصدر: Human Mutation.
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Mutant, CHO Cells, Deafness, Biology, medicine.disease_cause, Young Adult, 03 medical and health sciences, Cricetulus, Mutant protein, Cricetinae, Republic of Korea, Exome Sequencing, Genetics, medicine, Animals, Humans, Missense mutation, Genetics (clinical), Exome sequencing, Aged, Mutation, KCNQ Potassium Channels, Haplotype, Middle Aged, Pedigree, Potassium channel activity, Kinetics, Protein Subunits, HEK293 Cells, Phenotype, 030104 developmental biology, Child, Preschool, Female, Ion Channel Gating, KCNQ4